Biology subjects

Sona, D.

Publications and source records attributed to Sona, D..

3 recordsLinked to original sources

bioRxiv2020

Frequency-specific meso-scale structure of spontaneous oscillatory activity in the human brain

Recent studies provide novel insights into the meso-scale organization of the brain, highlighting the co-occurrence of different structures: classic assortative (modular), disassortative and core-periphery. However, the spectral properties of the brain meso-scale remain mostly unexplored. To fill this knowledge gap, we investigated how the meso-scale structure is organized across the frequency domain. We analyzed the resting state activity of healthy participants with source-localized high-density electroencephalography signals. Then, we inferred the community structure using weighted stochastic block-modelling to capture the landscape of meso-scale structures across the frequency domain. We found that meso-scale modalities were mixed over the frequency spectrum, with a core-periphery structure predominance. Nevertheless, we also highlighted a selective increase of disassortativity in the delta and theta bands, and of assortativity in the low gamma band (30-50 Hz). We further described other features of the meso-scale organization by identifying those brain regions which, at the same time, i) exhibited the highest degree of assortativity, disassortativity and core-peripheriness (i.e. participation), ii) were consistently assigned to the same community, irrespective from the granularity imposed by WSBM (i.e. granularity-invariance). We defined those brain areas as Participation and Granularity Invariant. In conclusion, we observed that the brain spontaneous activity shows frequency-specific meso-scale organization which may support spatially distributed and local information processing.

neuroscience↗

bioRxiv2018

Structurally Constrained Effective Brain Connectivity

The relationship between structure and function is of interest in many research fields involving the study of complex biological processes. In neuroscience in particular, the fusion of structural and functional data can help understanding the underlying principles of the operational networks in the brain. To address this issue, this paper proposes a constrained autoregressive model leading to a representation of "effective" connectivity that can be used to better understand how the structure modulates the function. Or simply, it can be used to find novel biomarkers characterizing groups of subjects. In practice, an initial structural connectivity representation is re-weighted to explain the functional co-activations. This is obtained by minimizing the reconstruction error of an autoregressive model constrained by the structural connectivity prior. The model has been designed to also include indirect connections, allowing to split direct and indirect components in the functional connectivity, and it can be used with raw and deconvoluted BOLD signal. The derived representation of dependencies was compared to the well known dynamic causal model, giving results closer to known ground-truth. Further evaluation of the proposed effective network was performed on two typical tasks. In a first experiment the direct functional dependencies were tested on a community detection problem, where the brain was partitioned using the effective networks across multiple subjects. In a second experiment the model was validated in a case-control task, which aimed at differentiating healthy subjects from individuals with autism spectrum disorder. Results showed that using effective connectivity leads to clusters better describing the functional interactions in the community detection task, while maintaining the original structural organization, and obtaining a better discrimination in the case-control classification task. HighlightsO_LIA method to combine structural and functional connectivity by using autoregressive model is proposed. C_LIO_LIThe autoregressive model is constrained by structural connectivity defining coefficients for Granger causality. C_LIO_LIThe usefulness of the generated effective connections is tested on simulations, ground-truth default mode network experiments, a classification and clustering task. C_LIO_LIThe method can be used for direct and indirect connections, and with raw and deconvoluted BOLD signal. C_LI

neuroscience↗

bioRxiv2018

Multi-Link Analysis: Brain Network Comparison via Sparse Connectivity Analysis

The analysis of the brain from a connectivity perspective is unveiling novel insights into brain structure and function. Discovery is, however, hindered by the lack of prior knowledge used to make hypotheses. On the other hand, exploratory data analysis is made complex by the high dimensionality of data. Indeed, in order to assess the effect of pathological states on brain networks, neuroscientists are often required to evaluate experimental effects in case-control studies, with hundreds of thousand connections.\n\nIn this paper, we propose an approach to identify the multivariate relationships in brain connections that characterise two distinct groups, hence permitting the investigators to immediately discover sub-networks that contain information about the differences between experimental groups. In particular, we are interested in data discovery related to connectomics, where the connections that characterize differences between two groups of subjects are found. Nevertheless, those connections not necessarily maximize accuracy in classification since this does not guarantee reliable interpretation of specific differences between groups. In practice, our method exploits recent machine learning techniques employing sparsity to deal with weighted networks describing the whole-brain macro connectivity. We evaluated our technique on functional and structural connectomes from human and mice brain data. In our experiments, we automatically identified disease-relevant connections in datasets with supervised and unsupervised anatomy-driven parcellation approaches, and by using high-dimensional datasets.

neuroscience↗